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Variant (rsID / SNP)

rs3746295

SLC1A6

rs3746295 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC1A6. Location: chromosome 19, position 15,083,693. The table records no clinical significance for this variant.

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Reference-table entries

SLC1A6Not classified
Variant type
synonymous_variant
Chromosome / position
19:15083693
HGVS
NM_001384669.1,c.30G>T,p.Leu10Leu
Allele change
Synonymous_L10L

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.